Golub E I, Garaev M M
Biokhimiia. 1975 Jan-Feb;40(1):25-31.
Analysis of E. coli W mutants defective in glucose transport suggests an existence of two enzyme systems which carry out the second step of phosphoenolpyruvate (PEP)-dependent glucose phosphorylation, thus controlling the glucose transport into E. coli cells. One system (PTS-glu-alpha) controls phosphorylation and transport of both glucose and alpha-methylglucoside, the other system (PTS-glu-beta) controls phosphorylation and transport of glucose only. PTS-glu-alpha system is damaged in the mutants studied, but PTS-glu-beta system is intact. On account of this fact the mutants do not uptake 14-C-alpha-methylglucoside and their extracts are practically incapable of its phosphorylation, phosphoenolpyruvate being used as phosphate donor. At the same time the mutants are capable of 14-C-glucose uptake and PEP-dependent 14-C-glucose phosphorylation. In one of the strain, having the intact PTS-glu-alpha system, the uptake of glucose and alpha-methylglucoside was stimulated by the addiction of glucose in the cultural medium. No such effect was observed in bacteria with the disturbed PTS-glu-alpha system and the intact PTS-glu-beta system. Probably, the PTS-glu-alpha system can be inducible, in contrast with the PTS-glu-beta system. The damage of the PTS-glu-alpha system results in resistance of bacteria to glucose-induced inhibition of the enzyme synthesis.
对葡萄糖转运有缺陷的大肠杆菌W突变体的分析表明,存在两种酶系统,它们执行磷酸烯醇丙酮酸(PEP)依赖性葡萄糖磷酸化的第二步,从而控制葡萄糖向大肠杆菌细胞内的转运。一个系统(PTS-葡萄糖-α)控制葡萄糖和α-甲基葡萄糖苷的磷酸化和转运,另一个系统(PTS-葡萄糖-β)仅控制葡萄糖的磷酸化和转运。在所研究的突变体中,PTS-葡萄糖-α系统受损,但PTS-葡萄糖-β系统完好无损。由于这一事实,突变体不摄取14-C-α-甲基葡萄糖苷,其提取物几乎不能将其磷酸化,磷酸烯醇丙酮酸用作磷酸盐供体。与此同时,突变体能够摄取14-C-葡萄糖并进行PEP依赖性的14-C-葡萄糖磷酸化。在一个具有完整PTS-葡萄糖-α系统的菌株中,培养基中添加葡萄糖会刺激葡萄糖和α-甲基葡萄糖苷的摄取。在PTS-葡萄糖-α系统受损而PTS-葡萄糖-β系统完好的细菌中未观察到这种效应。与PTS-葡萄糖-β系统相比,PTS-葡萄糖-α系统可能是可诱导的。PTS-葡萄糖-α系统的损伤导致细菌对葡萄糖诱导的酶合成抑制产生抗性。